Cas 143573-30-2,(1R,3S,5S,6R,10S)-10-Hydroxymethyl-3-phenyl-5-(2-propenyl)-2,4,7,9-tetraoxabicyclo<4.4.0>decane

143573-30-2

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Basic information

Product Name: (1R,3S,5S,6R,10S)-10-Hydroxymethyl-3-phenyl-5-(2-propenyl)-2,4,7,9-tetraoxabicyclo<4.4.0>decane
Synonyms:
CAS NO:143573-30-2
Molecular Formula:
Molecular Weight: 292.332
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (1R,3S,5S,6R,10S)-10-Hydroxymethyl-3-phenyl-5-(2-propenyl)-2,4,7,9-tetraoxabicyclo<4.4.0>decane(CAS DataBase Reference)
NIST Chemistry Reference: (1R,3S,5S,6R,10S)-10-Hydroxymethyl-3-phenyl-5-(2-propenyl)-2,4,7,9-tetraoxabicyclo<4.4.0>decane(143573-30-2)
EPA Substance Registry System: (1R,3S,5S,6R,10S)-10-Hydroxymethyl-3-phenyl-5-(2-propenyl)-2,4,7,9-tetraoxabicyclo<4.4.0>decane(143573-30-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 143573-30-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 143573-30-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,5,7 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 143573-30:
(8*1)+(7*4)+(6*3)+(5*5)+(4*7)+(3*3)+(2*3)+(1*0)=122
122 % 10 = 2
So 143573-30-2 is a valid CAS Registry Number.

143573-30-2Upstream product

143573-29-9 (1S,5R,6R,8R)-5-<(1S)-1-Hydroxy-3-butenyl>-8-phenyl-2,4,7,9-tetraoxabicyclo<4.4.0>decane

143573-30-2Downstream Products

143573-30-2Relevant academic research and scientific papers

Stereoselective formation of tetrahydrofurans during allyltrimethylsilane additions to L-xylose derivatives

Veloo, Ronald A.,Wanner, Martin J.,Koomen, Gerrit-Jan

, p. 5301 - 5316 (2007/10/02)

Stereoselective addition reactions to the aldehyde function of some L-xylose derivatives, under the influence of Lewis acid catalysts, lead to the formation of tetrahydrofuran derivatives at low temperatures, depending on the acetal protecting groups used

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